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General Information
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| Term |
aminoglycoside-induced deafness |
ID (Ontology) |
DOID:0111734 (Human Disease) |
| Definition |
A drug-induced hearing loss characterized by hearing loss induced by therapeutic doses of aminoglycoside antibiotics that has_material_basis_in mutation in the mitochondrial genes MTRNR1 or MTCO1 in combination with homozygous mutation in TRMU on chromosome 22q13.31. |
| Also Known As |
"streptomycin ototoxicity" ; "streptomycin-induced deafness" |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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aminoglycoside-induced deafness | 1 | for disease ribbon | aminoglycoside-induced deafness | 1 | model of | aminoglycoside-induced deafness | 1 |
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